{"title":"Diet restriction in parents shapes the lives of their offspring: a laboratory study using a predatory mite (Acari: Phytoseiidae)","authors":"Xiao Han, Keshi Zhang, Xia Chen, Zhi-Qiang Zhang","doi":"10.11158/saa.29.1.4","DOIUrl":null,"url":null,"abstract":"Environmental influences experienced by organisms are known to influence the phenotype of offspring through transgenerational plasticity or parental effects, and recent studies have revealed the significance of diet stress experienced by parents in shaping the life course of their progeny. In this laboratory study using a predatory mite, Phytoseiulus persimilis Athias-Henriot, we investigated the influence of parental diet restriction on offspring life history traits. We found that parental mites exposed to food reductions of 50% (Low diet) during both immature development and adult stages produced F1 offspring with reduced survival rates and fecundity compared to those from parents on abundant (High) diets. Sexually dimorphic responses emerged in response to parental diet restriction, whereby a reduced diet led to extended developmental periods for both male and female offspring while simultaneously reducing male size at maturity and increasing female size at maturity. We also found that diet restriction experienced by F0 individuals at both immature and adult stages manifested as reduced egg volumes and a less female-biased sex ratio in the F1’s offspring (i.e. the F2). There were additional significant interactions between the dietary history of parents and the dietary experiences of P. persimilis offspring themselves on various traits, including post-oviposition period, fecundity, and individual egg volume. These findings suggest that the dietary experiences of parents can modulate their offspring’s response when facing diet restriction. This study provided insights into non-genetic inheritance and transgenerational plasticity, highlighting the intricate interplay between environmental stressors and phenotypic responses.","PeriodicalId":51306,"journal":{"name":"Systematic and Applied Acarology","volume":"4 2","pages":""},"PeriodicalIF":1.3000,"publicationDate":"2024-01-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Systematic and Applied Acarology","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.11158/saa.29.1.4","RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENTOMOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Environmental influences experienced by organisms are known to influence the phenotype of offspring through transgenerational plasticity or parental effects, and recent studies have revealed the significance of diet stress experienced by parents in shaping the life course of their progeny. In this laboratory study using a predatory mite, Phytoseiulus persimilis Athias-Henriot, we investigated the influence of parental diet restriction on offspring life history traits. We found that parental mites exposed to food reductions of 50% (Low diet) during both immature development and adult stages produced F1 offspring with reduced survival rates and fecundity compared to those from parents on abundant (High) diets. Sexually dimorphic responses emerged in response to parental diet restriction, whereby a reduced diet led to extended developmental periods for both male and female offspring while simultaneously reducing male size at maturity and increasing female size at maturity. We also found that diet restriction experienced by F0 individuals at both immature and adult stages manifested as reduced egg volumes and a less female-biased sex ratio in the F1’s offspring (i.e. the F2). There were additional significant interactions between the dietary history of parents and the dietary experiences of P. persimilis offspring themselves on various traits, including post-oviposition period, fecundity, and individual egg volume. These findings suggest that the dietary experiences of parents can modulate their offspring’s response when facing diet restriction. This study provided insights into non-genetic inheritance and transgenerational plasticity, highlighting the intricate interplay between environmental stressors and phenotypic responses.
期刊介绍:
Systematic and Applied Acarology (SAA) is an international journal of the Systematic and Applied Acarology Society (SAAS). The journal is intended as a publication outlet for all acarologists in the world.
There is no page charge for publishing in SAA. If the authors have funds to publish, they can pay US$20 per page to enable their papers published for open access.
SAA publishes papers reporting results of original research on any aspects of mites and ticks. Due to the recent increase in submissions, SAA editors will be more selective in manuscript evaluation: (1) encouraging more high quality non-taxonomic papers to address the balance between taxonomic and non-taxonomic papers, and (2) discouraging single species description (see new special issues for single new species description) while giving priority to high quality systematic papers on comparative treatments and revisions of multiple taxa. In addition to review papers and research articles (over 4 printed pages), we welcome short correspondence (up to 4 printed pages) for condensed version of short papers, comments on other papers, data papers (with one table or figure) and short reviews or opinion pieces. The correspondence format will save space by omitting the abstract, key words, and major headings such as Introduction.